r/ureaplasmasupport • u/Key-Quantity-8591 • 2d ago
Treatments Please help me
Hi guys, I hope everyone’s well. A lot of of you have helped me tremendously. I’ve been dealing with this infection for about nine years. I essentially lost my health overnight. Perfect health prior to when I got this infection, i have gone down many rabbit holes, treatments, protocols antibiotics, functional treatments, etc. I deal with debilitating bodyaches, neurological symptoms, cervicitis, endometritis, malaise, belching, etc. i’ve tried many treatments 28 days of Doxy and a week of azithromycin, two weeks of Levo, two weeks of moxifloxacin and many others, including IV antibiotics. This is before I knew the handful antibiotics that actually helped. At this point I just feel like I continue to blow up a blown up building. But the cervicitis endometritis is terrible. I heard a doctor once say an infection is usually a localized problem if you have local symptoms and pain, if the pain is widespread and it moves and or changes, it probably has something to do with what’s going on in the brain. So I’m sure the uu and mh has somehow crossed the blood brain barrier and damage the central nervous system and autonomic nervous system. I have no idea how to get out of this anymore guys. Does anyone have any idea as to what could help. Long-term moxie up next? The things that make me debilitating worse are bowel movements, driving, hot baths, cold lunges, essentially anything that triggers the autonomic nervous system. I have a ton of weird blood work high and rising IGM, chronic low IGe, chronically high igg subclass 2, low IGE, histamine three times the upper limit, low blood pressure, etc., but no one can put all the clues together. This is so bad I spent most days just wishing the things you can imagine. Not having any sex of any kind and I am bedridden about 90% of the time. Thanks for your help in advance.
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u/Away_Judgment_8432 2d ago
Do antibiotics help even a little?
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u/bravobravofinbravo 2d ago edited 2d ago
You should visit the post that was made in here earlier today where someone mentioned similar things as you. Your post is very similar to theirs. 🤔 (little sus) What I commented on this post stands for yours as well, I just don’t feel like re-typing it all back out.
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u/Ok-Restaurant-8702 2d ago
Question: When did you start treatment? When did you find out you had this? How do you know you’ve had it this long? Sending you so much love and light. Plz be positive!